FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

SDU-700 PHASED ARRAY SECTOR AND LINEAR SCANNER

K Number: K873674 · Decision Oct 7, 1988
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
71
Applicant Total
49
Review Days
392

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Basic Information

Device Name
SDU-700 PHASED ARRAY SECTOR AND LINEAR SCANNER
K Number
K873674
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2880
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Shimadzu Corp.
Date Received
September 11, 1987
Decision Date
October 7, 1988
Product Code
JOP
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JOP Transducer, Ultrasonic

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